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流场流分级-电感耦合等离子体质谱法在细菌细胞悬浮液中铀结合研究中的应用。

Application of flow field flow fractionation-ICPMS for the study of uranium binding in bacterial cell suspensions.

作者信息

Jackson Brian P, Ranville James F, Neal Andrew L

机构信息

Savannah River Ecology Laboratory, University of Georgia, Aiken, South Carolina 29802, USA.

出版信息

Anal Chem. 2005 Mar 1;77(5):1393-7. doi: 10.1021/ac049278q.

Abstract

Field flow fractionation (FFF) is a size-based separation technique applicable to biomolecules, colloids, and bacteria in solution. When interfaced with ICPMS on-line, elemental data can be collected concurrent with size distribution. We employed hyperlayer flow FFF (Fl FFF) methodology to separate cells of Shewanella oneidensis strain MR-1 from exopolymers present in washed cell suspensions. With a channel flow of 4 mL min-1 and a cross-flow of 0.4 mL min-1 cells eluted with a retention time of 4.7 min corresponding to an approximate equivalent spherical cell diameter of 0.8 microm. Cell suspensions were amended with increasing concentrations of U to establish an adsorption isotherm and with fixed U concentrations at varying pH to establish the pH dependence of sorption. A linear sorption isotherm was determined for U solution concentrations of 0.2-16 microM, maximum U sorption occurred at pH 5. A high molecular weight compound, presumably a cell exudate, was identified by Fl FFF-ICPMS. This cell exudate complexed U, and at elevated pH, the exudate appeared to have a greater affinity for U than cell surfaces. Thus, Fl FFF interfaced with ICPMS detection is a powerful analytical technique for metal sorption studies with bacteria; analysis can be carried out on small sample volumes (25 microL) and additional speciation information can be gained because of the versatile Fl FFF separation range and multielement detection capabilities of ICPMS.

摘要

场流分级(FFF)是一种基于尺寸的分离技术,适用于溶液中的生物分子、胶体和细菌。当与电感耦合等离子体质谱仪(ICPMS)在线连接时,可以在收集尺寸分布数据的同时采集元素数据。我们采用超层流FFF(Fl FFF)方法,从洗涤后的细胞悬液中存在的胞外聚合物中分离出希瓦氏菌MR-1菌株的细胞。在通道流速为4 mL min⁻¹和错流流速为0.4 mL min⁻¹的条件下,细胞的保留时间为4.7分钟,洗脱出来的细胞对应的近似等效球形细胞直径为0.8微米。用浓度不断增加的铀对细胞悬液进行处理,以建立吸附等温线,并在不同pH值下用固定的铀浓度处理,以确定吸附的pH依赖性。在铀溶液浓度为0.2 - 16 microM时确定了线性吸附等温线,最大铀吸附发生在pH值为5时。通过Fl FFF - ICPMS鉴定出一种高分子量化合物,推测为细胞分泌物。这种细胞分泌物与铀络合,在较高pH值下,该分泌物对铀的亲和力似乎比细胞表面更大。因此,与ICPMS检测联用的Fl FFF是一种用于细菌金属吸附研究的强大分析技术;可以对小体积样品(25微升)进行分析,并且由于Fl FFF分离范围广泛以及ICPMS具有多元素检测能力,还可以获得额外的形态信息。

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